Medline MDSZOL100LORecalls & reported problems
Medline Industries, Inc. · PAD,DEFIB,ADULT,RADIOLUCENT,ZOLL,LO · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10888277635081), received between Sep 15, 2026 and Sep 16, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Connection Problem” (2 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Connection Problem2
- Communication or Transmission Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 16, 2026Communication or Transmission Problem; Connection Problem
It was reported that "These pads did not work with the customer's Zoll machines. They wouldn¿t recognize them or receive any signal like the OEM pads do."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50793034 ↗MalfunctionSep 15, 2026Connection Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50775650 ↗
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- Medline MDSPHY200Medline Industries, Inc. · Electrode, electrocardiograph, multi-function2 reports
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- Medline MDSZOL200Medline Industries, Inc. · Electrode, electrocardiograph, multi-function1 report
- Medline MDSPHY100LOMedline Industries, Inc. · Electrode, electrocardiograph, multi-function1 report
- Curaplex 16250Bound Tree Medical, LLC · Electrode, electrodcardiograph, multi-function1 report
- Medline MDSZOL200LOMedline Industries, Inc. · Electrode, electrocardiograph, multi-function1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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